Canonical Allele Identifier: PA2826149766
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 588359
ClinVar RCV Id: RCV002314452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171827.1:p.Gln785Pro
CA413251626
NM_001184898.2:c.2354A>C